A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18026730



Internal ID20593770
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:85787295..85790978hg38UCSC Ensembl
chr15:86330526..86334209hg19UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg383684
hg193684
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6515462
Supporting Variants
Samples
Known GenesKLHL25
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18026730
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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